Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

1,356 recalls, newest first

Class II · Moderate risk

Tadalafil Tablets

Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.

Terminated cGMP deviation Sun Pharmaceutical Industries INC NDC 16714-077-01 D-0231-2022
Class II · Moderate risk

Tadalafil Tablets

Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.

Terminated cGMP deviation Sun Pharmaceutical Industries INC NDC 16714-075-01 D-0230-2022
Class II · Moderate risk

Omeprazole Delayed-Release Capsules

CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.

Terminated cGMP deviation Dr. Reddy's Laboratories, Inc. NDC 70000-0232-1 D-0026-2022

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